[ccp4bb] Phoenix crystallisation robot

2016-10-27 Thread Inge Van Molle
Dear all,

We are looking for someone to take over our Art Robins Phoenix crystallisation 
robot, including the base module with 96 syringe head, wash module, nano module 
and humidifier chamber.
The robot was purchased in 2008 and is in perfect condition.

Please contact me for more information.
Price to be discussed.

Kind regards,

Inge




Dr. Inge Van Molle
VIB Structural Biology Research Center
Structural Biology Brussels
Vrije Universiteit Brussel
Building E, Pleinlaan 2, 1050 Brussel, Belgium

Tel 003226291859
Mobile 0032486521278






[ccp4bb] PhD position in structure-function studies of redox stress signaling proteins

2013-12-20 Thread Inge Van Molle
On behalf of Prof Joris Messens:














PhD position
in structure-function studies of redox stress signaling proteinsPosition: A PhD Research position is immediately available for
structure-function studies on peroxiredoxins of pathogentic Actinomycetes that
control signaling during oxidative stress. Successful candidates will join an
exciting research environment of the Messens VIB-laboratory in the Structural
Biology Research Center in Brussels. The Messens laboratory is recognized as a
world leader in the redox field, and the lab provides an outstanding position
in protein biochemistry and structure, in a highly dynamic and team-oriented
research group. Successful candidates will work on the FWO-project ‘A Combined
Experimental and Theoretical Approach towards Sulfenylation in the
Peroxiredoxin AhpE of M. tuberculosis:
Unraveling its Redox Chemistry’ in collaboration with the Frank De Proft lab at
the VUB, specialized in quantum chemical calculations, and with the Madia
Trujillo lab at Universidad de la República Uruguay. In this cutting-edge
research environment, you will tackle essential biological problems in oxidative
stress signaling and redox regulation.Project: Every 20 seconds a person dies from
tuberculosis (TB), which sums up to over 2 million deaths each year. Therefore,
the World Health Organization as well as the European Commission consider fighting
TB as one of the main goals for the coming years. The agent causing TB is Mycobacterium tuberculosis (Mtb). Mtb
infects, resides and multiplies in alveolar macrophages. Mtb causes the
formation of granulomas, where this pathogen is exposed to reactive oxygen
species (ROS) and reactive nitrogen species, which generate a toxic environment
aimed to kill the bacteria. Mtb engages advanced strategies to fight oxidative
stress. One of the key enzymes in the defence mechanism of Mtb is the one-cys
peroxiredoxin AhpE. AhpE scavenges ROS by its active site cysteine. In this
process, the cysteine is oxidized to the sulfenic acid. We will study how the
enzymatic environment influences the cysteine sulfenylation, and the
electron-transfer pathways in which AhpE is involved. We will use a
multidisciplinary approach involving structural and kinetic experiments, and
theoretical calculations to establish the rate determining structural
environment for cysteine sulfenylation. The moment we understand the details of
this ROS-scavenging enzyme, we might start to think about strategies to
interfere with this defense mechanism of Mtb.Requirements: Applicants should have obtained a Master
degree with a strong background and interest in protein biochemistry,
structural biology and enzymology. Candidates are expected to have strong work
ethics, excellent organization and communication skills, and critical thinking
abilities. We offer a friendly, enthusiastic and interactive environment. Our
staff is international and the working language is English. Please send a cover
letter discussing your interests in the laboratory and the project as well as
your CV and list of 3 individuals as references to joris.mess...@vib-vub.be.Kind regards,Inge


Dr. Inge Van MolleVIB,Structural Biology Research CenterOxidative Stress SignallingStructural Biology BrusselsVrije Universiteit BrusselBuilding E, room 4.16,Pleinlaan 2,1050 Brussel,BelgiumTel. 003226291992Mobile 0032486521278



[ccp4bb] Postdoctoral position in structure-function studies of redox stress signaling proteins

2013-12-08 Thread Inge Van Molle
On behalf of Prof. Joris Messens:

Postdoctoral position in structure-function studies of redox stress signaling 
proteins

 

Position: A postdoctoral Research position is immediately available for 
structure-function studies of plant proteins that control signaling during 
oxidative stress. Fellows will join an exciting research environment of the 
Messens VIB-laboratory in the Structural Biology Research Center in Brussels. 
The Messens laboratory is recognized as a world leader in the redox field, and 
the lab provides an outstanding position in protein biochemistry and structure, 
in a highly dynamic and team-oriented research group. Successful candidates 
will work on the FWO-project ‘The ROS-wave in plants: signaling along the 
sulfenome’ in collaboration with the Van Breusegem VIB-lab at Ugent, 
specialized in redox stress in plants. In this cutting-edge research 
environment of both labs, you will tackle essential biological problems in 
plant redox signaling.

 

Project: In plants, reactive oxygen species (ROS) are accumulated during 
abiotic and biotic stress (drought, extreme temperatures and various pathogen 
attacks), leading to severe crop yield losses worldwide due to their adverse 
effect on plant growth and development. However, tightly regulated, ROS act as 
signal transducers orchestrating plant development and metabolic adaptation to 
stress conditions. To get insights into these processes, we recently identified 
the sulfenome of plant cells under oxidative (H2O2) stress. The sulfenome is 
the set of proteins in which a cysteine thiol (-SH) is oxidized to a sulfenic 
acid (-SOH). These reversible post-transcriptional modifications function as 
“thiol-switches” which alter the biochemical properties of redox sensing 
proteins. Together with the Van Breusegem lab, we identified redox active 
proteins involved in signal transduction, redox homeostasis and a plethora of 
other metabolic pathways in plants.

In this project, we aim to establish a detailed structural and functional view 
of the mode of action of these redox proteins, in order to scrutinize their 
role in signaling during oxidative stress survival in plants.

 

Requirements: Applicants should have obtained a PhD in the last 5 years. 
Expertise with protein biochemistry and structural biology is essential. 
Knowledge of biophysical techniques and enzymology is an asset.

Please send a cover letter discussing your interests in the laboratory and the 
project as well as your CV and list of 3 individuals as references to 
joris.mess...@vib-vub.be.


Dr. Inge Van Molle
VIB, Department of Structural Biology
Structural Biology Brussels, Vrije Universiteit Brussel
Building E, room 4.16, Pleinlaan 2, 1050 Brussel, Belgium

Tel. 003226291992
Mobile 0032486521278



[ccp4bb] number of reflections in XDSCONV output file

2012-09-14 Thread Inge Van Molle
Dear all,

I have a question regarding the number of reflections in the output file of 
XDSCONV, given a number of reflections in the input file.

I have noticed that the number of reflections in the output file is only ~50% 
of the once accepted from the input file (ie the unique reflections)(input file 
is XSCALE.HKL or CORRECT_ASCII.HKL). This is in the case of FRIEDEL'S_LAW=FALSE:
SPACE_GROUP_NUMBER=   91
 UNIT_CELL_CONSTANTS=93.5793.57   364.05  90.000  90.000  90.000
 FRIEDEL'S_LAW=FALSE
 MERGE=TRUE 
 NUMBER OF REFLECTION RECORDS ON INPUT FILE  740375
 NUMBER OF IGNORED REFLECTIONS (I -3.0*SIGMA)0
 NUMBER OF REFLECTIONS ACCEPTED FROM INPUT FILE  106783

 NUMBER OF UNIQUE REFLECTIONS ASSIGNED TO TEST SET 2864
 NUMBER OF UNIQUE TEST REFLECTIONS INHERITED  0
 NUMBER OF UNIQUE TEST REFLECTIONS NEWLY GENERATED 2864

 NUMBER OF REFLECTION RECORDS ON OUTPUT FILE  57265
 NUMBER OF RECORDS ASSIGNED TO WORKING SET54401
 NUMBER OF RECORDS ASSIGNED TO TEST SET2864

In case FRIEDEL'S_LAW=TRUE, the number of unique reflections is just lower, and 
in the case the number of reflections in the output file does match the number 
of accepted reflections from the input file:
SPACE_GROUP_NUMBER=   91
 UNIT_CELL_CONSTANTS=93.5793.57   364.05  90.000  90.000  90.000
 FRIEDEL'S_LAW=TRUE 
 MERGE=TRUE 
 NUMBER OF REFLECTION RECORDS ON INPUT FILE  740115
 NUMBER OF IGNORED REFLECTIONS (I -3.0*SIGMA)0
 NUMBER OF REFLECTIONS ACCEPTED FROM INPUT FILE   57244

 NUMBER OF UNIQUE REFLECTIONS ASSIGNED TO TEST SET 2863
 NUMBER OF UNIQUE TEST REFLECTIONS INHERITED  0
 NUMBER OF UNIQUE TEST REFLECTIONS NEWLY GENERATED 2863

 NUMBER OF REFLECTION RECORDS ON OUTPUT FILE  57244
 NUMBER OF RECORDS ASSIGNED TO WORKING SET54381
 NUMBER OF RECORDS ASSIGNED TO TEST SET2863

For some reason, the outcome of having Friedel's law false or true is thus the 
same. Can anyone explain this to me? 
A colleague and I checked whether she sees the same using PointlessScala to 
get mtz file, and this has the same effect.

Kind regards,

Inge 

Dr. Inge Van Molle
Department of Chemistry
University of Cambridge
Lensfield Road
Cambridge
CB2 1EW

Tel 01223330190
iv...@cam.ac.uk


Re: [ccp4bb] Auto-Rickshaw: the EMBL-HH automated crystal structure determination platform

2008-04-15 Thread Inge Van Molle
Being one of those succesgul users I can say that this is great news!

Thanks Santosh,

Inge


 

-Original Message-
From: CCP4 bulletin board [mailto:[EMAIL PROTECTED] On Behalf Of
Santosh Panjikar
Sent: dinsdag 15 april 2008 9:45
To: CCP4BB@JISCMAIL.AC.UK
Subject: [ccp4bb] Auto-Rickshaw: the EMBL-HH automated crystal structure
determination platform

Dear Colleagues,

Have you ever heard of Auto-Rickshaw?

Auto-Rickshaw is the EMBL Hamburg automated structure determination
platform, which is now available as a web service. Try it out and solve your
structure in minutes.

The EMBL-Hamburg beamline user have been successfully using this system for
a little over three years. Now, for the new release with a lot of added
functionalities, we are happy to announce that Auto-Rickshaw can be accessed
by anybody in the Structural Biology community.

The Auto-Rickshaw phasing protocols include SAD, SIRAS, MAD, MR and MRSAD.
There are two versions: a beamline version and an advanced version.
The beamline version is geared towards speed so as to deliver the results in
the shortest amount of time whereas the advanced version can be used for
more complete model building if the resolution of the data permits.

For more detailed information visit
http://www.embl-hamburg.de/Auto-Rickshaw

The Auto-Rickshaw server is freely accessible to users who have the
necessary software licences. Academic usage requires free of charge
on-online registration at the same web site. Further inquiries can be made
to Santosh Panjikar at [EMAIL PROTECTED]


We would like to take this opportunity to thank all the developers of the
various crystallographic programs for their kind permission to invoke their
software within Auto-Rickshaw. We also gratefully acknowledge the feedback
from the EMBL-Hamburg beamline users and everybody who provided test data.


Santosh Panjikar on behalf of Auto-Rickshaw team

Auto-Rickshaw team
(Santosh Panjikar, Venkataraman Parthasarathy, Victor S. Lamzin, Manfred S.
Weiss and Paul A. Tucker)


Santosh Panjikar, Ph.D.  [EMAIL PROTECTED]
Staff Scientist
EMBL Hamburg outstation  http://www.embl-hamburg.de/~panjikar/
DESY, Notkestrasse 85Tel.:+49-40-89902-141
22603, Hamburg, Germany  Fax: +49-40-89902-149